Search results for "quantitative"

showing 10 items of 2409 documents

Supercritical Fluid Extraction and Supercritical Fluid Chromatography of Vitamin E in Pharmaceutical Preparations

1999

ChromatographyVitamine eChemistryGeneral Chemical EngineeringVitamin Emedicine.medical_treatmentSupercritical fluid extractionDosage formlaw.inventionlawSupercritical fluid chromatographymedicineFlame ionization detectorSample preparationQuantitative analysis (chemistry)Journal of High Resolution Chromatography
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Quantitative retention- and migration-toxicity relationships of phenoxy acid herbicides in micellar liquid chromatography and micellar electrokinetic…

2001

Abstract The need to obtain a tool for estimation of toxicity parameters for chemicals supports, the postulation of predictive models as an alternative to conventional classical assays. The use of micellar solutions of Brij35 as mobile phases in reversed phase liquid chromatography has proven to be valid in predicting some biological activities of different kinds of drugs. In this paper, the correlations between retention of phenoxy acids using different concentrations of Brij35 as micellar mobile phase in micellar liquid chromatography (MLC) and migration in micellar electrokinetic chromatography (MEKC) with several toxicity parameters are studied. Adequate correlations retention- and migr…

ChromatographybiologyChemistrymacromolecular substancesReversed-phase chromatographybiology.organism_classificationBiochemistryDaphniaMicellar electrokinetic chromatographyAnalytical ChemistryAquatic toxicologyMicellar liquid chromatographyMicellar solutionsEnvironmental ChemistryOrganic chemistryQuantitative analysis (chemistry)Chronic toxicitySpectroscopyAnalytica Chimica Acta
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Kinetic-Spectrophotometric Determination of Primary and Secondary Amines by Reaction with 1-2 Naphthoquinone-4-Sulphonate.

1994

Abstract A kinetic-spectrophotometric method for the determination of primary and secondary amines is described. It is based on the coloured reaction of these amines with sodium 1,2 Naphthoquinone 4-sulphonate (NQS) in the presence of a non-ionic surfactant. For each determination the optimum conditions were studied and found to be as follows: pH 10.5. Carbonate-bicarbonate buffer 0.1M, Triton X-100 0.1%, Temperature 45°C, and NQS 6.4 × 10−3 M and interval of time 45–180s at wavelength 490 nm. The parameters used for the quantitative determinations are the reaction rate and the increase in the absorbance of the kinetic curves. This procedure has been applied to the determination of ephedrin…

Chromatographymedicine.diagnostic_testBiochemistry (medical)Clinical BiochemistryNQSBiochemistryNaphthoquinoneAnalytical ChemistryReaction rateAbsorbancechemistry.chemical_compoundSulfonatechemistrySpectrophotometryElectrochemistrymedicineDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytical Letters
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Flow injection-spectrophotometric determination of metoclopramide hydrochloride.

1997

Abstract The determination of metoclopramide hydrochloride is spectrophotometrically determined by the Bratton-Marshall method in a flow injection assembly. The required nitrite is prepared on-line in the flow assembly by reducing a nitrate solution with the aid of a copperised cadmium solid-phase reactor. The calibration graph is linear over the range 0.5–85 mg l−1, with a relative standard deviation (RSD) of 0.89%, and sample throughput of 51 samples h−1. The method is easy and simple, and it is applied to determination of metoclopramide in some pharmaceutical formulations. The method eliminates the need for frequent preparation of unstable nitrite solutions.

Chromatographymedicine.diagnostic_testCalibration curveMetoclopramide HydrochlorideDosage formAnalytical Chemistrychemistry.chemical_compoundUltraviolet visible spectroscopyNitratechemistrySpectrophotometrymedicineNitriteQuantitative analysis (chemistry)Talanta
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Comparative Study on the Determination of Cephalexin in its Dosage Forms by Spectrophotometry and HPLC with UV-vis Detection

1997

This paper discusses the spectrophotometric determination of cephalexin as the intact cephalexin or as its acid-induced degradation product. Cephalexin can be determined in the range 1 × 10−5−18 × 10−5M with relative standard deviations of 5-1%. The limits of quantitation and detection were 10−5 and 0.3 × 10−5M, respectively. These procedures were compared with reversed-phase HPLC determination. No interference was observed in the presence of common pharmaceutical adjuvants. The H-point standard additions method was applied in order to correct for the possible presence of the cephalexin precursor, 7-aminocephalosporanic acid; this improves the selectivity of the UV-vis spectrophotometric me…

Chromatographymedicine.diagnostic_testChemistryHigh-performance liquid chromatographyDosage formAnalytical ChemistryUltraviolet visible spectroscopyCefalexinSpectrophotometryStandard additionmedicineQuantitative analysis (chemistry)medicine.drugAntibacterial agent
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Spectrophotometric determination of nalidixic and pipemidic acids in a flow injection assembly with a solid-phase reactor as a highly stable reagent …

2001

Abstract The flow-injection spectrophotometric determination of nalidixic (I) and pipemidic (II) acids were carried out by reaction with Fe(III) ions entrapped in a polymeric material and filling a packed-bed reactor; the released Fe(III) complexed with the quinolone is monitored at 426 nm. The method worked with a high reproducibility, even when using different reactors, days and solutions. Selectivity of the procedure was tested with different foreign compounds found in human urine as well as in pharmaceutical formulations containing both quinolones; no relevant interferences were observed. The calibration graph for (I) was linear over the range 1–250 μg ml −1 with a relative standard dev…

Chromatographymedicine.diagnostic_testNalidixic acidCalibration curveChemistryPipemidic acidBiochemistryDosage formAnalytical ChemistrySpectrophotometryReagentmedicineEnvironmental ChemistryQuantitative analysis (chemistry)SpectroscopyAntibacterial agentmedicine.drugAnalytica Chimica Acta
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Rapid and simultaneous high-performance liquid chromatography assay of polyamines and monoacetylpolyamines in biological specimens

2000

A rapid, resolutive and reproducible reversed-phase high-performance liquid chromatography (RP-HPLC) method was developed for polyamines and acetylpolyamines by adopting pre-column derivatization with benzoyl chloride. In a single run lasting less than 15 min ten polyamines were separated as well as traces of benzoic acid, methylbenzoate and benzoic anhydride. These contaminants, produced during the derivatization reaction, were almost all eliminated by washing steps envisaged in the same procedure. This simple and sensitive method can be applied to routine determination of polyamines in biological samples. A fine application of this procedure to the determination of endogenous content of p…

Chromatographymedicine.diagnostic_testorganic chemicalsBiogenic PolyaminesReproducibility of ResultsGeneral ChemistryReversed-phase chromatographyReference StandardsSensitivity and SpecificityHigh-performance liquid chromatographyBenzoic anhydridechemistry.chemical_compoundBenzoyl chloridechemistrySpectrophotometrymedicineSpectrophotometry UltravioletDerivatizationQuantitative analysis (chemistry)Chromatography High Pressure LiquidBenzoic acidJournal of Chromatography B: Biomedical Sciences and Applications
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Biopartitioning micellar chromatography to pedict mutagenicity of aromatic amines

2007

[EN] Mutagenicity is a toxicity endpoint associated with the chronic exposure to chemicals. Aromatic amines have considerable industrial and environmental importance due to their widespread use in industry and their mutagenic capacity. Biopartitioning micellar chromatography (BMC), a mode of micellar liquid chromatography that uses micellar mobile phases of Brij35 in adequate experimental conditions, has demonstrated to be useful in mimicking the drug partitioning process into biological systems. In this paper, the usefulness of BMC for predicting mutagenicity of aromatic amines is demonstrated. A multiple linear regression (MLR) model based on BMC retention data is proposed and compared wi…

Chronic exposureQuantitative structure–activity relationshipPredictive capabilityQuantitative Structure-Activity RelationshipAromatic aminesHigh-performance liquid chromatographyModels BiologicalMutagenicityDrug DiscoveryQUIMICA ANALITICAOrganic chemistryComputer SimulationAminesLeast-Squares AnalysisMicellesPharmacologychemistry.chemical_classificationChromatographyChromatographyOrganic ChemistryAromatic amineGeneral MedicineBiopartitioning micellar chromatographychemistryMicellar liquid chromatographyMutagenesisQuantitative retentione-activity relationships
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Identification and Detection of Phoma tracheiphila, Causal Agent of Citrus Mal Secco Disease, by Real-Time Polymerase Chain Reaction.

2006

Phoma tracheiphila is the causal agent of a tracheomycotic disease of citrus called mal secco causing the dieback of twigs and branches. This pathogen is of quarantine concern; therefore, fast and reliable protocols are required to detect it promptly. A specific primer pair and a dual-labeled fluorogenic probe were used in a real-time polymerase chain reaction (PCR) with the Cepheid Smart Cycler II System (Transportable Device TD configuration) to detect this fungus in citrus samples. Real-time PCR assay was compared to modified conventional PCR assay. The sensitivity of the former was evaluated by testing P. tracheiphila DNA dilutions, and the minimum amount detectable was about 500 fg, wh…

CitrusSerial dilutionPhoma tracheiphilaSettore AGR/12 - Patologia VegetaleCitrus limonFungusFungi imperfectiPlant ScienceBiologybiology.organism_classificationlaw.inventionMicrobiologyQuantitative PCRRutaceaeReal-time polymerase chain reactionCitrus; diagnostics; quantitative PCRlawdiagnosticsDiagnosticPathogenAgronomy and Crop SciencePolymerase chain reactionPlant disease
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Combining workload balance and patient priority maximisation in operating room planning through hierarchical multi-objective optimisation

2022

Abstract Previous analysis suggested the opportunity to consider the preferences of different stakeholders (hospital, patients, doctors and nurses) through the adoption of both patient priority maximisation and workload balance as performance criteria. The aim of this paper is to develop an effective and efficient solution approach for the operating room planning and scheduling capable to take into account the patient priority maximisation and workload balance criteria at the same time. This work is inspired by the need of a deeper understanding of the quality of the solutions obtained when a combination of the two criteria leads the OR planning decisions. Starting from a hierarchical multi…

Class (computer programming)Information Systems and ManagementGeneral Computer ScienceOperations researchExploitbusiness.industryComputer sciencemedia_common.quotation_subjectMatheuristics Operating room planning and scheduling OR in health servicesOperating room planning and schedulingOperating room managementWorkloadManagement Science and Operations ResearchIndustrial and Manufacturing EngineeringScheduling (computing)Quantitative analysis (finance)Modeling and SimulationMatheuristicsMatheuristics; Operating room planning and scheduling; OR in health servicesQuality (business)Local search (optimization)OR in health servicesSettore MAT/09 - Ricerca Operativabusinessmedia_common
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